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Distinct Metabolomic Signatures Are Associated with Longevity in Humans
Alterations in metabolism influence lifespan in experimental models, but data in humans are lacking. Here we use liquid chromatography/mass spectrometry to quantify 217 plasma metabolites and examine their relation to longevity in a large cohort of men and women. In 647 individuals followed for up t...
Autores principales: | , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4396657/ https://www.ncbi.nlm.nih.gov/pubmed/25864806 http://dx.doi.org/10.1038/ncomms7791 |
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author | Cheng, Susan Larson, Martin G. McCabe, Elizabeth L. Murabito, Joanne M. Rhee, Eugene P. Ho, Jennifer E. Jacques, Paul F. Ghorbani, Anahita Magnusson, Martin Souza, Amanda L. Deik, Amy A. Pierce, Kerry A. Bullock, Kevin O’Donnell, Christopher J. Melander, Olle Clish, Clary B. Vasan, Ramachandran S. Gerszten, Robert E. Wang, Thomas J. |
author_facet | Cheng, Susan Larson, Martin G. McCabe, Elizabeth L. Murabito, Joanne M. Rhee, Eugene P. Ho, Jennifer E. Jacques, Paul F. Ghorbani, Anahita Magnusson, Martin Souza, Amanda L. Deik, Amy A. Pierce, Kerry A. Bullock, Kevin O’Donnell, Christopher J. Melander, Olle Clish, Clary B. Vasan, Ramachandran S. Gerszten, Robert E. Wang, Thomas J. |
author_sort | Cheng, Susan |
collection | PubMed |
description | Alterations in metabolism influence lifespan in experimental models, but data in humans are lacking. Here we use liquid chromatography/mass spectrometry to quantify 217 plasma metabolites and examine their relation to longevity in a large cohort of men and women. In 647 individuals followed for up to 20 years, higher concentrations of the citric acid cycle intermediate, isocitrate, and the bile acid, taurocholate, are associated with lower odds of longevity, defined as attaining 80 years of age. In a larger cohort of 2,327 individuals with metabolite data available, higher concentrations of isocitrate but not taurocholate are also associated with worse cardiovascular health at baseline, as well as risk of future cardiovascular disease and death. None of the metabolites identified are associated with cancer risk. Our findings suggest that some, but not all, metabolic pathways to human longevity are dependent on modifying risk for the two most common causes of death. |
format | Online Article Text |
id | pubmed-4396657 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
record_format | MEDLINE/PubMed |
spelling | pubmed-43966572015-10-13 Distinct Metabolomic Signatures Are Associated with Longevity in Humans Cheng, Susan Larson, Martin G. McCabe, Elizabeth L. Murabito, Joanne M. Rhee, Eugene P. Ho, Jennifer E. Jacques, Paul F. Ghorbani, Anahita Magnusson, Martin Souza, Amanda L. Deik, Amy A. Pierce, Kerry A. Bullock, Kevin O’Donnell, Christopher J. Melander, Olle Clish, Clary B. Vasan, Ramachandran S. Gerszten, Robert E. Wang, Thomas J. Nat Commun Article Alterations in metabolism influence lifespan in experimental models, but data in humans are lacking. Here we use liquid chromatography/mass spectrometry to quantify 217 plasma metabolites and examine their relation to longevity in a large cohort of men and women. In 647 individuals followed for up to 20 years, higher concentrations of the citric acid cycle intermediate, isocitrate, and the bile acid, taurocholate, are associated with lower odds of longevity, defined as attaining 80 years of age. In a larger cohort of 2,327 individuals with metabolite data available, higher concentrations of isocitrate but not taurocholate are also associated with worse cardiovascular health at baseline, as well as risk of future cardiovascular disease and death. None of the metabolites identified are associated with cancer risk. Our findings suggest that some, but not all, metabolic pathways to human longevity are dependent on modifying risk for the two most common causes of death. 2015-04-13 /pmc/articles/PMC4396657/ /pubmed/25864806 http://dx.doi.org/10.1038/ncomms7791 Text en http://www.nature.com/authors/editorial_policies/license.html#terms Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use:http://www.nature.com/authors/editorial_policies/license.html#terms |
spellingShingle | Article Cheng, Susan Larson, Martin G. McCabe, Elizabeth L. Murabito, Joanne M. Rhee, Eugene P. Ho, Jennifer E. Jacques, Paul F. Ghorbani, Anahita Magnusson, Martin Souza, Amanda L. Deik, Amy A. Pierce, Kerry A. Bullock, Kevin O’Donnell, Christopher J. Melander, Olle Clish, Clary B. Vasan, Ramachandran S. Gerszten, Robert E. Wang, Thomas J. Distinct Metabolomic Signatures Are Associated with Longevity in Humans |
title | Distinct Metabolomic Signatures Are Associated with Longevity in Humans |
title_full | Distinct Metabolomic Signatures Are Associated with Longevity in Humans |
title_fullStr | Distinct Metabolomic Signatures Are Associated with Longevity in Humans |
title_full_unstemmed | Distinct Metabolomic Signatures Are Associated with Longevity in Humans |
title_short | Distinct Metabolomic Signatures Are Associated with Longevity in Humans |
title_sort | distinct metabolomic signatures are associated with longevity in humans |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4396657/ https://www.ncbi.nlm.nih.gov/pubmed/25864806 http://dx.doi.org/10.1038/ncomms7791 |
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